SNAINSTITUTEOFPHARMA
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Oct 07, 2024
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About This Presentation
dosage form
Size: 1.78 MB
Language: en
Added: Oct 07, 2024
Slides: 33 pages
Slide Content
Pharmaceutical Dosage Forms
By
Himani Jaisinghani
What is Pharmaceutical Dosage Forms
A dosage form is a pharmaceutical preparation
consisting of drug and excipients to facilitate dosing,
administration, and delivery of the content to the drug
product.
The design, materials, manufacturing, and testing of all
dosage forms target drug product quality. A testing
protocol must consider not only the physical,
chemical, microbiological, and biological properties of
the dosage form as appropriate, but also the
administration route and desired dosing regimen.
List of official dosage forms
•Aerosols
•Capsules
•Creams
•Emulsions
•Films
•Foams
•Gases
•Gels
•Granules
•Gums
•Implants
List of official dosage forms
•Injections
•Inserts
•Shampoos
•Soaps
•Solutions
•Sprays
•Strips
•Suppositories
List of official dosage forms
•Suspensions
•Tablets
•Liquids
•Lotions
•Ointments
•Pastes
•Pills
•Powders
Dose Uniformity
Consistency in dosing for a patient or consumer requires
that the variation in the drug substance content of each
dosage unit be accurately controlled throughout the
manufactured batch or compounded lot of drug product.
Uniformity of dosage units typically is demonstrated by
one of two procedures: content uniformity or weight
variation.
Stability
Drug product stability involves the evaluation of
chemical stability, physical stability, and performance
over time.
For tablets, capsules, oral suspensions, and implants, in
vitro release test procedures such as dissolution and
disintegration provide a measure of continuing
consistency in performance over time.
Bioavailability
Bioavailability is influenced by factors such as the method of
manufacture or compounding, particle size, crystal form (polymorph)
of the drug substance, the properties of the excipients used to formulate
the dosage form, and physical changes as the drug product ages.
With proper justification, in vitro release testing (e.g., disintegration
and dissolution) may be used as a surrogate to demonstrate consistent
availability of the drug substance from the formulated dosage.
Dosage Form/ Drug Delivery
System by route of administration
Oral
Tablets
Capsules
Solutions
Syrups
Elixirs
Suspensions
Gels
Powders
Sublingual
Tablets
Lozenges
Parenteral
Solutions
Suspensions
Conjunctival
Contact lens inserts
Ointments
Dosage Form/ Drug Delivery
System by route of administration
Epicutaneous /
transdermal
Ointments
Creams
Infusion pumps
Pastes
Plasters
Powders
Aerosols
Lotions
Intraocular
Solutions
Suspensions
Intranasal
Solutions
Sprays
Inhalers
Ointments
Intrarespiratory
Aerosols
Dosage Form/ Drug Delivery
System by route of administration
Vaginal
Solutions
Ointments
Emulsion foams
Gels
Tablets
Inserts,
suppositories
Rectal
Solutions
Ointments
Suppositories
Urethral
Solutions
suppositories
Solid Dosage Forms
Powders and Granules
Capsules and Tablets
Oral Liquid Dosage Forms
Oral solutions
Syrups
Elixirs
Tinctures
Example of Syrup
Antihistamine Syrup
1.Chlorpheniramine maleate 0.4g
2.Glycerin 25.0ml
3.Syrup base 83.0 ml
4.Sorbitol solution 283 ml
5.Sodium Bezoate 1.0 g
6.Alcohol 60.0 ml
7.Color and Flavor q.s.
8.Purified water to make 1000.0ml
Disperse Systems
Suspensions
Emulsions
Aerosols
Sterile Dosage Forms and
Delivery Systems
Parenterals
Biologicals
Ophthalmic solutions and
suspensions